CA2956939A1 - Novel corrosion inhibition package - Google Patents

Abstract

A corrosion inhibition package for use with an aqueous acid composition, said package comprising: a terpene;a cinnamaldehyde or a derivative thereof; at least one amphoteric surfactant; and a solvent. Also disclosed are compositions comprising said corrosion inhibitor package. Preferably, the corrosion inhibition package meets the environmental requirements for classification as yellow according to the Norwegian North Sea offshore drilling regulatory requirements.

Description

NOVEL CORROSION INHIBITION PACKAGE
FIELD OF THE INVENTION
This invention relates to corrosion inhibition packages for use with acidic compositions, more specifically to corrosion inhibition packages which provide an enhanced environmentally-friendly characteristic while still providing industry-leading corrosion protection.
BACKGROUND OF THE INVENTION
In the oil & gas industry, stimulation with an acid is performed on a well to increase or restore production. In some instances, a well initially exhibits low permeability, and stimulation is employed to commence production from the reservoir. In other instances, stimulation or remediation is used to further encourage permeability and flow from an already existing well that has become under-productive.
Acidizing is a type of stimulation treatment which is performed above or below the reservoir fracture pressure in an effort to restore or increase the natural permeability of the reservoir rock. Acidizing is achieved by pumping acid into the well to dissolve typically limestone, dolomite and calcite cement between the sediment grains of the reservoir rocks or to treat acid soluble scale accumulation.
There are three major types of acid applications: matrix acidizing, fracture acid izing, and breakdown acidizing (pumped prior to a fracturing pad or cement operation in order to assist with formation breakdown (reduce fracture pressures, increased feed rates), as well as clean up left over cement in the well bore or perforations. A matrix acid treatment is performed when acid is pumped into the well and into the pores of the reservoir formation below the fracture pressure. In this form of acidization, the acids dissolve the sediments formation and/or mud solids that are inhibiting the permeability of the rock, enlarging the natural pores of the reservoir while creating wormholes and stimulating flow of hydrocarbons to the wellbore. While matrix acidizing is when pressures are maintained below the fracture gradient, fracture acidizing involves pumping highly pressurized acid into the well above the formation fracture gradient, physically fracturing the reservoir rock allowing the acid to etch the permeability inhibitive sediments. This type of acid treatment forms channels or fractures and etches through which the hydrocarbons can flow. In some instances, a proppant is introduced into the fluid which assists in propping open the fractures, further enhancing the flow of hydrocarbons into the wellbore.

There are many different mineral and organic acids used to perform an acid treatment on wells. The most common type of acid employed on wells to stimulate production is hydrochloric acid (HC1), which is useful in stimulating carbonate reservoirs.
Some of the major challenges faced in the oil & gas offshore industry from using hydrochloric acid include the following: extremely high levels of corrosion (which is countered by the addition of 'filming' type corrosion inhibitors that are typically themselves toxic and harmful to humans, the environment and equipment and thus affect the classification rating or use in many offshore jurisdictions (such as the North Sea). Reactions between acids and various types of metals can vary greatly but softer metals, such as aluminum and magnesium, are very susceptible to major effects causing immediate damage. Hydrochloric acid produces Hydrogen chloride gas which is toxic (potentially fatal) and corrosive to skin, eyes and metals.
At levels above 50 ppm (parts per million) it can be Immediately Dangerous to Life and Health (IDHL). At levels from 1300-2000 ppm death can occur in 2-3 minutes.
The inherent negative effects (organic sterility, poisoning of wildlife, personnel exposure, high corrosion, hazardous fumes etc.) of HCI and the corrosion inhibitors added to reduce this corrosion in the event of an unintended or accidental release on surface or down hole into water aquifers or other sources of water are devastating which can cause significant pH reduction of such and can substantially increase the toxicity and could potentially cause a mass culling of aquatic species and potential poisoning of humans or livestock and wildlife exposed to/or drinking the water. An unintended release at surface can also cause a hydrogen chloride gas plume to be released, potentially endangering human and animal health. This is a common event at large storage sites when tanks split or leak. Typically if near the public, large areas need to be evacuated post event and a comprehensive, expensive to implement, emergency evacuation plan need to be in place prior to approval of such storage areas. Because of its acidic nature, hydrogen chloride gas is also corrosive, particularly in the presence of moisture. A method to overcome gas fuming is by using novel synthetic acids which have an ability to control this drawback all the while maintaining the efficiency of the acid downhole.
The inability for acids and blends of such to biodegrade naturally without neutralizing the soil results in expensive cleanup-reclamation costs for the operator should an unintended release occur. Moreover, the toxic fumes produced by mineral & some organic acids are harmful to humans/animals and are highly corrosive and/or produce potentially explosive vapours. Transportation and storage requirements for acids are restrictive and taxing in such that you must haul the products in acid approved tankers or intermediate bulk containers (IBC) that are rated to handle such corrosive products. As well, the dangers surrounding exposure by personnel handling the blending of such corrosive/dangerous products limits their

2 use/implementation. Some if not most of these problems have been greatly minimized through the use of synthetic acids as mentioned above.
Another concern is the potential for exposure incidents on locations due to high corrosion levels of acids causing storage container failures and/or deployment equipment failures i.e. coiled tubing or fracturing iron failures caused by high corrosion rates (pitting, cracks, pinholes and major failures). Other concerns include: downhole equipment failures from corrosion causing the operator to have to execute a work-over and replace down hole pumps, tubing, cables, packers etc.; inconsistent strength or quality level of mineral &
organic acids; potential supply issues based on industrial output levels; high levels of corrosion on surface pumping equipment resulting in expensive repair and maintenance levels for operators and service companies; the requirement of specialized equipment that is purpose built to pump acids greatly increasing the capital expenditures of operators and service companies; and the inability to source a finished product locally or very near its end use; transportation and onsite storage difficulties.
Extremely high corrosion and reaction rates with temperature increase causes conventional acids to "spend/react or become neutral" prior to achieving its desired effect such as deeply penetrating an oil or gas formation to increase the wormhole or etched "pathway" effectively to allow the petroleum product to flow freely to the wellbore. As an example, hydrochloric acid can be utilized in an attempt to free stuck drill pipe in some situations. Prior to getting to the required depth to dissolve the formation that has caused the pipe/tubing to become stuck many acids spend or neutralize due to increased bottom hole temperatures and greatly increased reaction rate, so it is advantageous to have an alternative that spends or reacts more methodically allowing the slough to be treated with a solution that is still active, allowing the pipe/tubing to be pulled free.
When used to treat scaling issues on surface due to water contamination, conventional acids are exposed to human and mechanical devices as well as expensive pumping equipment causing increased risk for the operator and corrosion effects that damage equipment and create hazardous fumes. When mixed with bases or higher pH fluids, acids will create a large amount of thermal energy (exothermic reaction) causing potential safety concerns and equipment damage, acids typically need to be blended with fresh water (due to their intolerance of highly saline water, causing potential precipitation of minerals) to the desired concentration requiring companies to pre-blend off-site as opposed to blending on-site with field/produced water thereby increasing costs associated with transportation.
Conventional mineral acids used in a pH control situation can cause rapid degradation of certain polymers/additives requiring increased loadings or chemicals to be added to counter these negative effects.

3 Many offshore areas of operations have very strict regulatory rules regarding the transportation/handling and deployment of acids causing increased liability and costs for the operator.
When using an acid to pickle tubing or pipe, very careful attention must be paid to the process due to high levels of corrosion, as temperatures increase, the typical additives used to control corrosion levels in acid systems begin to degrade very quickly (due to the inhibitors "plating out" on the steel) causing the acids to become very corrosive and resulting in damage to downhole equipment/tubulars.
Acids perform many actions in the oil & gas industry and are considered necessary to achieve the desired production of various petroleum wells, maintain their respective systems and aid in certain drilling operational functions (i.e. freeing stuck pipe, filter cake treatments). The associated dangers that come with using mineral acids are expansive and tasking to mitigate through controls whether they are chemically or mechanically engineered. Eliminating or even simply reducing the negative effects of acids while maintaining their usefulness is a struggle for the industry. As the public demand for the use of cleaner/safer/greener products increases, companies are looking for alternatives that perform the required function without all or most of the drawbacks associated with the use of conventional acids. Some of the problems raised above have been greatly mitigated through the implementation and use of novel synthetic acids. However, even some of those synthetic acid compositions comprise certain chemicals which prohibit their use in certain environments.
Offshore oil and gas operations are highly regulated due to the environmental concerns which arise from their operations and the potential for spills. The complexity of drilling and completing offshore wells is compounded by both safety issues for workers on such offshore oil rigs and production platforms as well as environmental concerns.
Many countries bordering the waters where offshore drilling and production is routinely carried out have put into play a number of regulations aimed at minimizing the environmental impact of this practice.
These regulations include the ban on certain types of chemicals which may be harmful to marine life and the environment. In order to overcome these very restrictive regulations, many oil companies employ very costly containment programs for the handling of certain chemicals such as acids which have a wide array of uses in the industry of oil and gas exploration and production.
Norwegian offshore drilling regulations are amongst the most stringent on the planet. The regulatory authorities routinely carry out monitoring of the water column in each of the 11 offshore regions of Norwegian waters.

4 This monitoring involves the measurement and tracking of pollutants or biological effects of pollutants, using caged or wild-caught organisms. This allows the regulatory authorities to assess the impact of offshore drilling on the marine fauna. In concert with these intense regulatory monitoring activities, the approval of offshore chemicals is another aspect that is intensely controlled.
In addition to the water column monitoring, the regulatory body takes sediment samples from the seabed to assess the pollution which does not enter fishes and other organisms. These physical and chemical sediment testing seek to quantify: the total organic matter (TOM); grain sin distribution; hydrocarbons and synthetic drilling fluids; metals; and radioactivity.
The chemicals are classified according three main criteria: persistence (lack of biodegradation, liability to bioaccumulate and toxicity.
Many of the issues related with offshore oil and gas exploration and production stem from the fact that the conditions under which this is carried out are substantially different than those encountered in the same types of operations carried out onshore.
Acidic compositions conventionally used in various oil and gas operations can reach temperatures of up to and above 130 C. At these temperatures, their reactivity is exponentially increased and, as such, their effectiveness or even their ability to be utilized is greatly decreased.
Corrosion is the major concern at high temperatures and is difficult and expensive to control with additional chemistry.
Modified and synthetic acids developed and currently patented are aimed at increasing personnel safety, reducing corrosion effects, reducing environmental damage, retarding the reaction and diffusion rate, increasing worm-holing efficiency (reducing competing wormholes) and reducing the toxicity profile of 14C1.
Additionally, there is the risk of wellbore and/or formation damage due to uncontrolled solubilized mineral precipitation due to an increase in the pH caused mainly by the formation of ammonia during the decomposition phase. The advent of newer synthetic or modified acids is intended on providing usage at higher temperatures while still maintain the performance, safety and environmental advantages and benefits of a urea-HC1 modified or synthetic acid system, but ultimately at these higher temperatures it is most often necessary to utilize additional or purpose developed corrosion inhibition packages and/or components to control corrosion of exposed steel. In that respect, even short exposure times at high temperature are more damaging to steel than longer exposure times at lower temperatures. In keeping with the changing times, there is also a strong desire to develop corrosion packages which are more "environmentally friendly and more effective" than conventional packages.

5 EP patent application 1 724 375 A2 discloses an aqueous organic acid composition containing a terpene as corrosion inhibitor intensifier said to be especially suitable for use in acidizing subterranean formations and wellbores. The composition is said to substantially reduce the corrosive effects of the acidic solution on metals in contact with the acidic solution. Suitable terpenes are said to include carotene, limonene, pinene, farnesene, camphor, cymene and menthol.
US patent no. 8,765,021 teaches an aqueous treatment composition for inhibiting corrosion and acid attack on metallic surfaces that comprises a thiourea organic derivative, a polyalkoxylated terpene nonionic ' surfactant and an acid. The invention also relates to a process for cleaning industrial metallic equipment, in particular heat exchangers in which a heat transfer fluid, generally based on air or on water, flows, with a view to cleaning them and removing scale and other soiling.
US patent application no. 2003/0166472 discloses a well treatment microemulsion that is formed by combining a solvent-surfactant blend with a carrier fluid. In preferred embodiments, the solvent-surfactant blend includes a surfactant and a solvent selected from the group consisting of terpenes and alkyl or aryl esters of short chain alcohols. The disclosed well treatment microemulsion can be used in well remediation, stimulation and hydrogen sulfide mitigation operations.
US patent no. 8,323,417 teaches a method of treatment for inhibiting sulfur-based corrosion or scaling or for removing scaling from a surface including inhibiting corrosion caused by sulfur-containing materials, reducing corrosion caused by sulfur-containing materials, inhibiting scaling caused by sulfur-containing materials in gas, liquid or solid phase or any combination of multiple phases of materials, reducing scaling caused by sulfur-containing materials, and removing scaling caused by sulfur-containing materials. The method involves contacting sulfur-containing materials with a composition containing a turpentine liquid, wherein said turpentine liquid comprises a-terpineol, p-terpineol, 3-pinene, and p-cymene.
US patent application no. 2006/0264335 Al discloses an aqueous organic acid composition containing a terpene as corrosion inhibitor intensifier is especially suitable for use in acidizing subterranean formations and wellbores. The composition substantially reduces the corrosive effects of the acidic solution on metals in contact with the acidic solution. Suitable terpenes are said to include carotene, limonene, pinene, farnesene, camphor, cymene and menthol.
US 9,074,289 B2 discloses a method of inhibiting corrosion of a surface in contact with a corrosive environment encountered in oil and gas operations. The method includes contacting the surface with a

6 composition comprising a quaternary nitrogen-containing corrosion inhibitor.
The patent teaches the use of such inhibitor at levels ranging from 0.1 to 8%.
Despite the various known corrosion inhibition packages, there is still a need for corrosion inhibition packages for use with HCI, modified and synthetic acid compositions in the oil industry which can be used over a range of applications, that are formulated to be useful for synthetic and modified acid systems and still be effective with conventional acids such as HCI and can be used at high temperatures (i.e. ¨130 C) without having its components degrade, phase out of solution and have a superior safety and environmental profile over known packages during use at those temperatures. Moreover, it is desirable to have corrosion inhibition packages that do not undermine the advantages of environmentally and personnel-friendly acid compositions such as various synthetic and modified acid compositions which have fewer deleterious effects than typical conventional mineral and some organic acids.
Certain corrosion inhibitors such as propargyl alcohol are undesirable in offshore application such as in the North Sea as it is rated red and moreover has a poor performance on Cr-13 alloys since it tends to pit the surface. Surfactants are desirable when used in combination with corrosion inhibitors bnt they also carry their own set of issues, as they have in general a high acute fish toxicity and lower biodegradability (less than 60% in seawater). In tight of those drawbacks, short chain non-ionic surfactants are typically preferred, because they typically exhibit better acute fish toxicity. However, a disadvantage of short chain non-ionic surfactants is that they usually have lower dispersion ability. Therefore, it is much more difficult and, in some cases, not possible to disperse a relatively hydrophobic corrosion inhibition component (such as citral or also cinnamaldehyde or other terpenes) with a nonionic surfactant.
It was unexpectedly discovered that the corrosion inhibition packages according to the present invention exhibit stability when combined with acidic compositions under exposure to elevated temperature (up to and above 130 C). This consequently makes them useful in various industries using acids at these temperatures including, but not limited to, the oil and gas industry.
SUMMARY OF THE INVENTION
According to a first aspect of the present invention, there is provided a corrosion inhibition package for use with an aqueous acid composition, said package comprising:
- a terpene;
- a cinnamaldehyde or a derivative thereof;
- at least one amphoteric surfactant; and

7 - a solvent.
Preferably, the corrosion inhibition package according to the present invention is comprised of components giving it an environmental classification in Norwegian waters of at least "Yellow". According to a preferred embodiment the corrosion inhibition package has a "Gold"
classification for UK waters. Also preferably, the corrosion inhibition package has a classification of "R" in Dutch waters.
Preferably, the terpene is selected from the group consisting of: citral;
ionone; ocimene; carvone; and cymene. A preferred terpene is citral.
Preferably, the at least one amphoteric surfactant is selected from the group consisting of: a sultaine surfactant; a betaine surfactant; and combinations thereof. More preferably, the sultaine surfactant and betaine surfactant are selected from the gaup consisting of: an amido betaine surfactant; an amido sultaine surfactant; and combinations thereof. Yet even more preferably, the amido betaine surfactant and is selected from the group consisting of: an amido betaine comprising a hydrophobic tail from C8 to C16. Most preferably, the amido betaine comprising a hydrophobic tail from C8 to C16 is cocamidobetaine.
The inventors have unexpectedly discovered that a specific surfactant class that is rated yellow for North Sea applications can also provide very good dissolution of corrosion inhibitors with loading ranges that make it economically feasible to use. This class of surfactant, amido betaines, allow the production of a stable dispersion of the terpene component in acid without phase separation, with a yellow rating.
Preferably also, the corrosion inhibition package further comprises an anionic surfactant. Preferably, the anionic surfactant is a carboxylic surfactant. More preferably, the carboxylic surfactant is a dicarboxylic surfactant. Even more preferably, the dicarboxylic surfactant comprises a hydrophobic tail ranging from C8 to C16. Most preferably, the dicarboxylic surfactant is sodium latiriminodipropionate Preferably, the surfactant is selected from the group consisting of:
cocamidopropyl betaine; 13-Alanine, N-(2-carboxyethyl)-N-dodecyl-, sodium salt (1:1); and a combination thereof.
Preferably, the solvent is selected from the group consisting of: methanol;
ethanol; isopropanol;
ethylene glycol; and 2-butoxyethanol; and combinations thereof. A preferred solvent is methanol.

8 Preferably, the terpene is present in an amount ranging from 2% to 25% by weight of the total weight of the corrosion inhibition package. Preferably also, the at least one surfactant is present in an amount ranging from 2% to 20% by volume of the total weight of the corrosion inhibition package. Preferably also, the solvent is present in an amount ranging from 25% to 80%, more preferably from 25% to 75% by volume of the total weight of the corrosion inhibition package.
According to another aspect of the present invention, there is provided an acidic composition comprising:
- an acid;
- a corrosion package comprising:
- a terpene;
- a cinnamaldehyde or a derivative thereof;
- at least one surfactant; and - a solvent;
wherein the volume % of the corrosion package in the acidic composition ranges from 0.1 to 7.5%.
Preferably, the acidic composition further comprises a metal iodide or iodate.
Preferably the weight/volume % of the metal iodide or iodate in the acidic composition ranges from 0.1 to 1.5%. More preferably, the wt/vol. % of the metal iodide or iodate in the acidic composition ranges from 0.25 to 1.25%. Even more preferably, the wt/vol. % of the metal iodide or iodate in the acidic composition is approximately 1%. Preferably, the metal iodide or iodate selected from the group consisting of: cuprous iodide; potassium iodide; sodium iodide; lithium iodide and combinations thereof. More preferably, the metal iodide is potassium iodide.
According to one aspect of the present invention, there is provided an acidic composition comprising a corrosion inhibition package according to the invention and an acid selected from the group consisting of:
mineral acids; organic acids, synthetic acids; and combinations thereof. More preferably, the acid is selected from the group consisting of: HCI; Lysine-HCI; Urea-HCI; hydrofluoric acid;
sulfuric acid; phosphoric acid;
phosphoric acid-urea; p-toluene sulfonic acid; methanesulfonic acid; and methanesulfonic acid-urea. Even more preferably, the acid is HCI, Urea-HCI or lysine-HCI.
According to an aspect of the present invention, there is provided an aqueous synthetic acid composition for use in onshore oil and gas operations, said composition comprising: lysine and hydrochloric acid in a molar ratio of not less than 1:12; a surfactant; a corrosion inhibitor; and an intensifier. Preferably,

9 not less than 1:8, more preferably 1:5. According to another preferred embodiment, the ratio is of not less than 1:3.
According to an aspect of the present invention, there is provided an aqueous synthetic acid composition for use in offshore oil and gas operations, said composition comprising: urea and hydrochloric acid in a molar ratio of not less than 0.1:1; a corrosion inhibitor; and an intensifier. More preferably, the ratio is not less than 0.3:1, even more preferably, the ratio is not less that 0.5:1, yet even more preferably the ratio is not less than 0.7:1.
The use of a corrosion inhibitor package with an acidic composition where the acidic composition comprises an acid selected from the group consisting of: a mineral acid; an organic acid or a synthetic acid, said corrosion inhibitor package comprising:
- a terpene;
- a cinnamaldehyde or a derivative thereof;
- at least one amphoteric surfactant; and - a solvent.
According to another aspect of the present invention, there is provided a use of a synthetic or modified acid composition comprising a preferred embodiment of the corrosion inhibition package according to the present invention in the oil and gas industry to perform an activity selected from the group consisting of: stimulating formations; assisting in reducing breakdown pressures during downhole pumping operations;
treating wellbore filter cake post drilling operations; assisting in freeing stuck pipe; descaling pipelines and/or production wells; increasing injectivity of injection wells; lowering the pH of a fluid; fracturing wells; performing matrix stimulations; conducting annular and bullhead squeezes & soaks; pickling tubing, pipe and/or coiled tubing; increasing effective permeability of formations;
reducing or removing wellbore damage; cleaning perforations, nozzles, ports, jets etc.; solubilizing limestone, dolomite, and calcite; and removing undesirable scale, unassisted or natural high formation temperature production wells, injection wells and their related surface and down-hole equipment and facilities at temperatures up to 130 C.
According to another aspect of the present invention, there is provided a synthetic or modified acid composition comprising a corrosion inhibition package according to a preferred embodiment for use in the oil and gas industry which has high salinity tolerance. A tolerance for high salinity fluids, or brines, can be desirable for offshore acid applications. Conventional acids are normally blended with fresh water and additives, typically far offsite, and then transported to the area of treatment as a finished blend. In certain instances it may prove advantageous to have an alternative that can be transported as a concentrate safely to the treatment area, then blended with a saline produced water or sea water greatly reducing the logistics requirement. A conventional acid composition can precipitate salts/minerals heavily if blended with fluids of an excessive saline level resulting in formation plugging or ancillary damage, inhibiting production and substantially increasing costs. Brines are also typically present in formations, thus having an acidic composition system that has a high tolerance for brines greatly reduces the potential for formation damage or emulsions forming down-hole during or after product placement/spending (reaction) occurs.
A preferred embodiment of the present invention provides a corrosion inhibition package which provides various oilfield grade steel alloys exceptional protection against corrosion when exposed to acidic compositions at low to high temperatures (upwards of 130 C). Additionally, the components used in the preferred corrosion inhibition package are quite environmentally friendly.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
The description that follows, and the embodiments described therein, is provided by way of illustration of an example, or examples, of particular embodiments of the principles of the present invention.
These examples are provided for the purposes of explanation, and not limitation, of those principles and of the invention.
According to an aspect of the invention, there is provided a corrosion inhibition package for use with an acidic composition which will be placed in contact with a metallic surface, said corrosion inhibition package comprising:
- a terpene;
- cinnamaldehyde or a derivative thereof;
- at least one amphoteric surfactant; and - a solvent.
=
Preferably, the corrosion inhibition package is used with an acidic composition such as a synthetic acid composition comprising:
- lysine & hydrogen chloride in a molar ratio of not less than 1:12;
preferably in a molar ratio not less than 1:8, more preferably in a molar ratio of not less than 1:5, even more preferably in a molar ratio of not less than 1:3 and even more preferably in a molar ratio of not less than 1:2.5.

According to another preferred embodiment, the corrosion inhibition package is used with an acidic composition such as a synthetic acid composition comprising: urea and hydrogen chloride in a molar ratio of not less than 0.1:1; more preferably in the urea and hydrogen chloride are present in a molar ratio of not less than 0.5:1; yet more preferably in the urea and hydrogen chloride are present in a molar ratio of not less than 0.7:1, and even more preferably in the urea and hydrogen chloride are present in a molar ratio of not less than 1:1.
Preferably, when the synthetic or modified acid composition comprises lysine and hydrogen chloride, the molar ratio of lysine to HC1 can range from 1:2 to 1:12;
preferably in a molar ratio ranging from 1:2.5 to 1:8, more preferably in a molar ratio ranging from 1:3 to 1:6, even more preferably in a molar ratio ranging from 1:3 to 1:5.
The terpenes considered by the inventors to achieve desirable corrosion inhibition results comprise:
monoterpenes (acyclic); monocyclic terpenes; and beta-1onone. Exemplary but non-limiting compounds of some of the previously listed terpene sub-classes comprise: for monoterpenes:
citral (mixture of geranial and neral); citronellal; geraniol; and ocimene; for monocyclic terpenes: alpha-terpinenc; carvone; p-cymene.
More preferably, the terpenes are selected from the group consisting of:
citral; ionone; ocimene; and cymene.
According to a preferred embodiment of the present invention, the corrosion inhibition package comprises a surfactant which is environmentally friendly. More preferably, the surfactant is capable of withstanding exposure to temperatures of up to least 130 C for a period of 2 to 4 hours in a closed environment without undergoing degradation.
Preferably, the at least one amphoteric surfactant is selected from the group consisting of: a sultaine surfactant; a betaine surfactant; and combinations thereof. More preferably, the sultaine surfactant and betaine surfactant are selected from the group consisting of: an amido betaine surfactant; an amido sultaine surfactant; and combinations thereof. Yet even more preferably, the amido betaine surfactant and is selected from the group consisting of: an amido betaine comprising a hydrophobic tail from C8 to C16. Most preferably, the amido betaine comprising a hydrophobic tail from C8 to C16 is cocamidobetaine.
Preferably, the cinnamaldehyde derivative are selected from the group consisting of:
dicinnamaldehyde p-hydroxycinnamaldehyde; p-methylcinnamaldehyde; p-ethylcinnamaldehyde; p-methoxyc innamaldehyde;
p-dimethylam noc nnama I dehyde; p- d iethylam inocinnam al dehyd e; p-nitrocirinamaldehyde; o-nitrocinnamaldehyde; 4-(3-properial)cinnamaldehyde; p-sodium sulfocinnamaldehyde p- trimethylammoniumcinnamaldehyde sulfate; p-trimethylammoniumcinnamaldehyde o- methylsulfate; p-thiocyanocinnamaldehyde;
p-(S-acetypthiocinnamaldellyde; p-(S-N,N-dimethylcarbamoylthio)cinnamaldehyde; p-ch lorocinnamaldehyde; a- methy I c nnamaldehyde ; p-methyleinnamaidehyde; a-chlorocinnamaldehyde a- bromocinnamaldehyde; a-butylcinriamaldehyde; a-amylcinnamaldehyde; a- hexylcinnarnaldehyde; ct-bromo-p-cyanocinnamaldehyde; a-ethyl-p-methylcinnamaldelvde and p-methyl-a-pcntylcinnamaldehyde.
Preferably also, the corrosion inhibition package further comprises an anionic surfactant. Preferably, the anionic surfactant is a carboxylic surfactant. More preferably, the carboxylic surfactant is a dicarboxylic surfactant. Even more preferably, the dicarboxylic surfactant comprises a hydrophobic tail ranging from C8 to C16. Most preferably, the dicarboxylic surfactant is sodium lauriminodipropionate A preferred embodiment can refer to a corrosion inhibition package comprising cocamidopropyl betaine and 13-Alanine, N-(2-carboxyethyl)-N-dodecyl-, sodium salt (1:1).
According to a preferred embodiment of the present invention, when preparing an acidic composition comprising a corrosion inhibition package, metal iodides or iodates such as potassium iodide, sodium iodide, cuprous iodide and lithium iodide can be added as corrosion inhibitor intensifier. The iodide or iodate is preferably present in a weight/volume percentage ranging from 0.1 to 1.5%, more preferably from 0.25 to 1.25%, yet even more preferably I% by weight/volume of the acidic composition. Most preferably, the iodide used is potassium iodide. According to a preferred embodiment, chlorides such as aluminum chloride, calcium chloride, bismuth chloride and magnesium chloride can be used instead of metal iodides or iodates as intensifiers.
According to a preferred embodiment of the present invention, the corrosion package comprises:
cocamidopropyl betaine in an amount of approximately 5% by volume of the total volume of the package;
Citral in an amount of approximately 10 % by volume of the total volume of the package; cinnamaldehyde in an amount of approximately 10 % by volume of the total volume of the package;
and methanol in an amount of approximately 75% by volume of the total volume of the package.
According to a preferred method of use, the corrosion inhibitor package is mixed with an acid prior to its transport to a job site. Alternatively, a corrosion inhibitor package according to the present invention can be mixed with the acid prior to its use while using proper mixing equipment and mixing the combined composition thoroughly to ensure homogenous mixing.

=
Example 1 - Process to prepare an acidic composition comprising a corrosion inhibition package according to a preferred embodiment of the invention Lysine mono-hydrochloride is used as starting reagent. To obtain a 1:2 molar ratio of lysine to HC1, 370 ml of 50 wt% lysine-HC1 solution and 200 ml HC1 aq. 36% (22 Baume) were combined. The corrosion inhibition package, and potassium iodide are added at this point. Circulation is maintained until all products have been solubilized. Additional products can now be added as required.
The corrosion inhibiton package is prepared by dispersing a terpene component in methanol, and at least one surfactant. Afterwards, the corrosion inhibition package thus prepared is mixed with an acidic composition. Applying this procedure, allows for the formation of a surfactant complex as described below.
According to a preferred embodiment of the present invention, since the corrosion inhibition package is intended for use at high temperatures, the combination of a betaine and a carboxylic surfactant is desirable.
The combination of a carboxylic surfactant and a betaine is known to form a 1:1 or 1:2 complex, which has also a high molecular weight. Therefore, it is important to disperse the terpene component into isopropanol.
Otherwise, the resulting acidic composition may not meet the class I fluid (transparent, no phase separation).
The resulting composition of Example 1 is an amber-colored liquid with a fermentation-like odour having an expected shelf-life of greater than a year. It has a freezing point temperature of approximately minus 45 C and a boiling point temperature of approximately 100 C. It has a specific gravity of 1.15 0.02. It is completely soluble in water and its pH is less than 1.
The composition is biodegradable and is classified as a mild irritant according to the classifications for skin tests. The composition is substantially low fuming. Toxicity testing was calculated using surrogate information and the LD50 was determined to be greater than 2000mg/kg.
With respect to the corrosion impact of the acidic composition on typical oilfield grade steel alloys, it was established that it was clearly well below the acceptable corrosion limits set by industry making it highly desirable as corrosion is the main challenge during acid applications causing substantial maintenance and workover costs over time.
Corrosion inhibition package formulations Various types of steel alloy coupons were subjected to corrosion testing in the presence of conventional, synthetic and modified acid compositions using corrosion inhibitor components according to preferred embodiments of the present invention at various temperatures. The results of the corrosion tests are reported in Tables 3 through 23. Coupons of various grades of steel alloys (indicated in each table) were exposed to the various listed compositions for varying duration periods at varying temperatures.
According to preferred embodiment of the present invention, citral can be present in a concentration ranging from 5 to 30%; cinnamaldehyde can be present in a concentration ranging from 5 to 30%; and cocamido betaine can be present in a concentration ranging from 2.5 to 15%.
Depending on various factors, such as temperature, acid, metal, etc. preferred corrosion inhibitor package loadings within the acid compositions can range between 0.1 to 7.5% vol/vol. Biodegradation, toxicity and bioaccumulation testing carried out has indicated that most of the compositions listed below in Tables 1 and 2 have been identified as satisfactorily meeting the requirements for listing under a classification of Yellow for offshore use in the North Sea (Norway).
Table 1 ¨ List of Component and Content in Corrosion Inhibition Packages FCI-XV to FCI-XP
(All figures are in vol %) Compound Cocamidopropyl betaine 10 10 10 10 5 5 10 B -Alanine, N-(2-carboxyethyl)-N-dodecyl-, 10 sodium salt (I :1) Citral 10 20 25 25 25 25 25 Cinnamaldehyde 25 10 10 10 Carvone 10 Methanol 80 70 40 55 60 60 45 Total vol. % 100 100 100 100 100 100 Table 2¨ List of Component and Content in Corrosion Inhibition Packages FCI-XN
to FCIAK
(All figures are in vol %) Name FCI-XN FCI-XM _ FCI-XL FCI-XI FCI-XJ FCI-XK
Cocamidopropyl betaine 10 5 5 10 5 5 B.-Alanine, N-(2-carboxyethyl)-N-dodecyl-, 10 5 10 5 sodium salt (1: I ) Cita] 10 10 10 15 15 15 Cinnamaldehyde 10 10 10 10 10 10 Carvone Methanol 60 75 70 55 70 65 Total vol. to 100 100 100 100 100 100 Corrosion testing The following corrosion testing outlined in the tables below for a number of different corrosion inhibition packages according to the present invention in the presence of a synthetic or modified acid composition was carried out diluted with saline water at various temperatures for various durations of exposure. A desirable result was one where the 1h/ft2 corrosion number is at or below 0.05. More desirable is that the corrosion (in lb/ft2) is at or below 0.02.
The following abbreviations are used in the corrosion results tables: Cl-IA -

10% KI solution; ZA ¨
Cinnamaldehyde; and CA ¨ Citral. HCR-2000N is a proprietary blend synthetic acid comprising HC1. HCR-3000N is a proprietary blend synthetic acid comprising methanesulfonic acid.
HCR-6000N is a proprietary blend synthetic acid comprising HC1.
Table #3¨ Corrosion test results from tests conducted at 90 C for a period ranging for 6 hours with a coupon density of 7.86 g/cc having a surface area of 41.4 cm2 (coupons used were 1018 steel) mc""r L'-11)111;
-= '.1 Diluted in HCR-2000N 50% seawater 0,168 296.053 7.52 0.008 1%1% ZA CI-1A
Diluted in HCR-2000N 50% seawater 1% FCI-XT0.54 954.5765 24.246 0.027 1% CI-IA
Diluted in 1.50/0 FC1-XT
HCR-2000N 50% seawater 0.439 775.1076 19.688 0.022 1% CI-1A
Diluted in HCR-2000N 50% seawater 1% FCI-XS 0.18 318.6632 8.094 0.009 1%CI-1A
Diluted in 1% FCI-XS
HCR-2000N 50% seawater 0.5% CI-1A 0.238 420.7626 10.687 0.012 Diluted in 1.50/0 FCI-XS
HCR-2000N 50% seawater 0,151 266.9069 6.779 0,007 1% CI-1A
1.50/0 FCI-XS
HCR-2000N Diluted in 0.185 327.4953 8.318 0.009 0.5% C1-1A

50% seawater Diluted in 2.50/0 FC1-XS
HCR-2000N 50% seawater 0.124 218.6835 5.555 0.006 1% CI-IA
Diluted in % FCI-XS 2.5 HCR-2000N 50% seawater 0.149 263.904 6.703 0.007 0.5% CI-1A
Diluted in HCR-2000N 50% seawater 0.235 415.2867 10.548 0.012 1% CI-1A
Diluted in 1.5% 1C1-XR
HCR-2000N 50% seawater 0.153 270.6164 6.874 0.008 1% CI-1A
Diluted in HCR-2000N 50% seawater 1% FCI-XQ0.274 484.3539 12.303 0.014 1% CI-1A
Diluted in 1% FCI-XQ
HCR-2000N 50% seawater 0.341 602.5278 15.304 0.017 0.5% C1-1A
Diluted in CI-X

HCR-2000N 50% seawater . 5% F 0.18 318.1333 8.081 0.009 I% CI-1A
Diluted in CI-HCR-2000N 50% seawater 1.5% F XQ0.255 450.0853

11.432 0.013 0.5% C1-1A
Diluted in 1% Fa-xR
HCR-2000N 50% seawater 0 0 0 I% CI-1A
Diluted in 1-ICR-2000N 50% seawater 0.312 551.3015 14.003 0.015 0.5% CI-1A
Diluted in 1.50/0 FC1-XR
HCR-2000N 50% seawater 0.182 321.6661 8.17 0.009 1% CI-1A
Diluted in 1.5% 5% FCI-1A CI-XR
El-CR-2000N 50% seawater 0.213 375.7188 9.543 0.011 0.
Table #4 - Corrosion test results from tests conducted at 110 C for a period ranging for 6 hours with a coupon density of 7.86 g/cc having a surface area of 41.4 cm2 (coupons used were 1018 steel) r=:; ' - mi , r I .40V t etStVdi AYI;a " A
Diluted :50%
1.5% FCI-XQ
I-ICR-3000N seawater 0.125 220.8032 5.608 0.006 1% CI-IA
Diluted in 50%
1.5% - XRFCI
HCR-3000N seawater 0.1 176.4659 4.482 0.005 1% CI-1A

Diluted in 50% 1.5% FC1-XS
HCR-3000N seawater 0.081 143.6104 3.648 0.004 1 A, C1-1A
Diluted in 50% 1.56}C1-.XT' HCR-3000N seawater1.073 1895.022 48.134 0.053 1% CI-IA
Diluted in 50% 1 .5% FC1-XP
HCR-3000N seawater 0.048 85.49501 2.172 0.002 1% CI-1A
Table #5- Corrosion test results from tests conducted at 90 C for a period ranging for 6 hours with a coupon density of 7.86 g/cc having a surface area of 41.4 cm2 (coupons used were 1018 steel) ________________ ' '42.,44111t1oss=''Mil11:1171)Y"r - =
=
Diluted in 50% I% FCI-XS
HCR-2000N seawater 0.171 301.3522 7.654 0.008 1% CI-1A
Diluted in 50%
1% FCI-XS
HCR-2000N seawater 0.226 399.9188 10.158 0.011 0.5% CI-1A
Diluted in 50%
HCR-2000N seawater 1.5 /0 C1-1A FC1-XS
1%
0.127 224.6894 5.707 0.006 Diluted in 50%
HCR-2000N seawater 1.5% FCI-XS
0.147 260.3712 6.613 0.007 0.5% CI-IA
Table #6 - Corrosion test results from tests conducted at 130 C for a period ranging for 6 hours with a coupon density of 7.86 g/cc having a surface area of 41.4 cm2 (coupons used were 1018 steel) OlisOiSolv 'Ormqvar WM."
_ iSit6 f = ;r-*
Diluted in 50%
1.5% FC1-XQ
HCR-3000N seawater 1% C1-1A 2.249 3971.808 100.884 0.111 Diluted in 50%
1.5% FCI-XR.
HCR-3000N seawater 1.763 3114.032 79.096 0.087 1%C1-1A
Diluted in 50%
1,5%FCI-XS
HCR-3000N seawater 0.237 418.8195 10.638 0.012 1% CI-1A
Diluted in 50% 1.5% FCI-XT
HCR-3000N seawater 1% CI-1A 2.849 5032.37 127.822 0.141 HCR-3000N Diluted in 50% 1.5% FC1-XP 0.114 201.9025 5.128 0.006 , seawater 1% CI-1A
Table #7¨ Corrosion test results from tests conducted at 90 C for a period ranging for 4 or 6 hours with a coupon density of 7.86 g/cc having a surface area of 26.01 cm2 (coupons used were CR-13410 polished) ,, ,,,,.-,,,A,Q,;,., ,,õ,:: .,'..7.
µ`..i..;.:n 2, . ,:-..,,,...H:f.517,-.....,' -: ,:j,,,,,''' !F,,..,,,Arsi.i, ' ' ,,,,,;''''=,:k: '';''-, q=C-.. i',Pr,r,;T..4.; .C. ' :I, 10'itr:I. *OW' nfE,IrEt i7.; '2:- liAlda.,,,..:.' .. OPP! rcer !.1µ-t''.''',,lf,-.1.1'!
ImPru-7" ' . ' . 4 1 c .-s -'' .7 ' :
Diluted in 50%
H 5% FC1-XR
CR-2000N seawater 0.66 4 2785.604 70.754 0.044 5% C1-1A
- Diluted in 50%

HCR-2000N seawater 5)/0FCI-XP0.459 4 1934.108 49.126 0.03 5% CI-IA

Table #8 ¨ Corrosion test results from tests conducted at 70 C for a period ranging for 6 hours with a coupon density of 7.86 g/cc having a surface area of 41.4 cm2 (coupons used were 1018 steel) It -;-,' ''. ,' 10,1");' if' ' ' g : ': ' "..;.:.*r ,,42_,,,`,..i,ilf..f,,:.,,:,?: , ,,-,, Diluted in 50%
1% FCI-XQ
HCR-2000N seawater 0.076 133.3651 3.387 0.004 1% CI-IA
' Diluted in 50%
1% FC1-XQ
HCR-2000N seawater 0.5% C1-1A 0.09 158.2717 4.02 0.004 -Diluted in 50%
HCR-2000N seawater 1.5% FCI-XQ
0.076 133.5418 3.392 0.004 1% CI-1A
Diluted in 50%
1.5% FCI-XQ
0.087 153.679 3.903 0.004 HCR-2000N seawater 0.5% CI-1A
_ Diluted in 50%
1% FCI-XR
HCR-2000N seawater 1% C1-1A 0.081 142.3739 3.616 0.004 Diluted in 50%

HCR-2000N seawater 0.5% C1-1A 0.097 171.1667 4.348 0.005 -Diluted in 50%
HCR-2000N seawater 1.5% FC1-XR
0.076 133.5418 3.392 0.004 1% CI-IA
Diluted in 50%
HCR-2000N seawater 1.5% FCI-XR
0.5% CI-1A 0.091 160.7447 4.083 0.005 Diluted in 50%
HCR-2000N seawater 1% FCI-XS
0.077 136.0148 3.455 0.004 1% CI-1A
Diluted in 50%
1% FCI-XS
HCR-2000N seawater 0.5%
0.097 =170.8134 4.339 0.005 Diluted in 50%
HCR-2000N seawater 1.5% FCI-XS
0.065 114.9943 2.921 0.003 1% C1-1A
Diluted in 50%
FICR-2000N seawater 1.5% FCI-XS
0.07 124.0031 3.15 0.003 0.5% C1-1A
Table #9- Corrosion test results from tests conducted at 110 C for a period ranging for 6 hours with a coupon density of 7.86 g/cc having a surface area of 41.4 cm2 (coupons used were 1018 steel) 'Y. ' Mit tosS.;-';',.'.
Diluted in 50%
1.5%
HCR-6000N seawater FCI-XQ
0.463 817.5018 20.765 0.023 1% C1-1A
Diluted in 50%
HCR-6000N seawater 1.5% FCI-XR
0.176 311.4209 7.91 0.009 1% CI-1A
Diluted in 50%
1.5% FCI-XS
0.157 276.6223 7.026 0.008 HCR-6000N seawater 1% CI IA
Diluted in 50% 1.50/
HCR-6000N seawater o FC1-XP
0.238 421.1159 10.696 0.012 1% C1-1A
Diluted in 50%
HCR-6000N seawater 1.5% FCI-XT
1.12 1978.927 50.265 0.055 1% CI-IA
Table #10- Corrosion test results from tests conducted at 90 C for a period ranging for 6 hours with a coupon density of 7.86 g/cc having a surface area of 28.922 cm2 (coupons used were J55 steel) õ _____________________________________________ =xir . = -, ...
-,41613servatiuns 7-'. =
Ati'e-Vez l';17fieRi.,7'.1:t1 7 -7.5% HC1 None 1.404 j 3550.3032 90.178 0.100 15% HC1 None 2.175 5500.3023 139.708 0.154 Diluted in 1.5% FC1-XP
HCR-2000N 50% seawater 1% C1-1A 0,119 300.3889 7.63 0.008 no pits HCR-2000N Diluted in 1.5% FCI-XQ
0.218 551.4715 14.007 0.015 no pits I% C1-1A

50% seawater Diluted in 5% FC1-XR
HCR-2000N 50% seawater 1. 0.216 546.6673 13.885 0.015 no pits 1%C1-1A
Diluted in 5%
HCR-2000N 50% seawater 1 .% FCI-XS 0.186 470.8115 11.959 0.013 no pits Table #11¨ Corrosion test results from tests conducted at 90 C for a period ranging for 6 hours with a coupon density of 7.86 g/cc having a surface area of 30.199 cm2 (coupons used were N80 steel) ______________________________________________________________________ , __ exe, -..e005010.4::y . on,nc_", = I
:raccirag, .J.
(control) none 0.117 304,9971 7.747 0.009 Diluted in 50%
HC1-Urea none 0.370 963.1762 24,465 0.027 seawater Diluted in 50% 1.5% FCI-XP few pits on HCR-2000N 0.128 310.2075 7,879 0.009 seawater 1% C1-1A
side/tack Diluted in 50%
HCR awater 1.5% FCI-XQ -2000N 0.278 672.4795 17.081 0.019 no pits se 1% CI-1A
Diluted j50 " 1.5% FCI-XR
HCR-2000N 0.247 598.3784 15.199 0.017 no pits seawater 1% CI-IA
Diluted in 50%
H.CR-2000N seawater 1.5% FCI-XS 0.206 500.0613 12.702 0.014 no pits 1% CI-1A
Table #12 ¨ Corrosion test results from tests conducted at 90 C for a period ranging for 6 hours with a coupon density of 7.86 g/cc having a surface area of 30.199 cm2 (coupons used were L80 steel) a-- .
'W:f10 S -1100:
_ ;==== .-õArtFseelita. wins Diluted in 1.5% FCI-XP
few pits on HCR-2000N 50% seawater 0.153 369.779 9.392 0.01 1% CI-1A
side/back Diluted in 1.1% 50/o Cl IA

FCI-XQ
HCR-2000N 50% seawater =0.289 698.875 17.751 0.02 no pits , , Diluted in 1.5%FCI-XR
HCR-2000N 50% seawater 0.296 716.0684 18.188 0.02 no pits 1% CI-lA
-Diluted in 1.5% FCI-XS
14CR-2000N 50% seawater 0.232 562.5387 14.288 0.016 no pits 1% CI-1A
Table #13 - Corrosion test results from tests conducted at 90 C for a period ranging for 6 hours with a coupon density of 7.86 g/cc having a surface area of 28.922 cm2 (coupons used were P110 steel) ,.-...,... ,,,..c' ,-IK::-. ',:'õ'''... :, -.=:..' :.1>., *iiiiiiii mm/
year '. -'..' ': .:* -2 .4year, ., ibr ._;'..: ; .1* *-i),.i. i.
i Diluted in 50%
HCR-2000N seawater 1.5% FCI-XP
1% CI-1A 1.575 3983.187 101.173 0.078 no pits Diluted in 50%
1.5%
HCR-2000N seawater FCI-XQ
0.645 1630.141 41.406 0.046 pYitsesOnsosliTidees 1% C1-1A
Diluted in 50%
HCR-2000N seawater 1.5 /o FCI-XR Yes, some 0.77 1945.954 49.427 0.055 1% CI-1A pits on sides _ Diluted in 50%
1.5% FCI-XS
I-JCR-2000N seawater 10/ Cl IA 0.387 978.5395 24.855 0.027 no pits Table #14- Corrosion test results from tests conducted at 130 C for a periodranging for 6 hours with a coupon density of 7.86 g/cc having a surface area of 28.922 cm z (coupons used were 1018 steel) ' ' Stlifiee'..,. ''.' - .5'i . !.:-,`... ''.. , a tivear 1hf '. ,.,4;:ijiv.'''q'',-- ' -,',-.';`.,.'''.,µ:.--_:c,":
i:;:':;,...Eg,11",t111),:::. ''':-,.:--'','',,.. :.::...'.4).444 ": '-7417,4s49",,',..... .:.i- '; ' :---:=/...,:..'%:.;'==
.',:_., , ..F54 .4i4.54t;s4C,'13 , :-., .',;-.: .'": ;.
..,4:ii.f...111fIrgO'''.';.'..: . µ:,/,,:- SIO,'-' ' '''' ::`,:':41i) :1' ' ' -'" ':':: ' :=\. l'-..:' : ', : - , :- ' - - 7' Diluted in 500/0 HCR-6000N seawater 1.5% FCI-XQ
1.399 28.922 3537.913 89.863 0.099 1%C1-1A
Diluted in 50%
1.50/o FCI-XR
HCR-6000N seawater 1% CI-1A 1.114 41.4 1966.915 49.96 0.055 Diluted in 50%
1.5% FC1-XS
HCR-6000N seawater 1% CI-1A 0.336 41.4 592.8125 15.057 0.017 , Diluted in 50%

HCR-6000N seawater l.

- 3.839 41.4 6780.955 172.236 0.19 1 /o C1-1A
FICR-6000N Diluted in 50% 1.5% FCI-XP 0.315 41.4 556.4241 14.133 0.016 seawater 1% CI-1A
Table #15 - Corrosion test results from tests conducted at 90 C for a period ranging in for 6 hours with a coupon density of 7.86 g/cc having a surface area of 41.4 cm 2(coupons used were 1018 steel) *Am- aniiyearli/ftPack =
- , Cl-XP
1.5%
15% HC1 0.075 132.8352 3.374 0.004 1% CI-1A
2.5% FCI-XP
15% HCI 0.068 119.587 3.038 0.003 1% CI-1A
1.5% FCI-XQ
15% NCI 1.121 1980.693 50.31 0.055 1% C1-1A
2.5% FCI-XQ
15% HC1 0.793 1400.069 35.562 0.039 1% C1-1A
1.5% FCI-XR
15% HCI 0.176 310.8909 7.897 0.009 1% CI-1 A
2.5%
15% HC1 FCI-XR0.215 380.4881 9.664 0.011 I% CI-1A
1.5% FCI-XS
15% HC1 0.2 353.2851 8.973 0.01 1% C1-1A
2.5% FCI-XS
15% HC1 0.228 402.2151 10.216 0.011 1% CI-1A
Table #16- Corrosion test results from tests conducted at 90 C for a period ranging for 6 hours with a coupon density of 7.86 Wee having a surface area of 30.199 cm` (coupons used were L80 steel) 4,44-ils/$41,-' '16 Diluted in 1.5%5/ FC1-1XP few pits on 0.
2000N 50% seawater 0.18 435.6466 11.065 0.012 Side/back ')0 CI-A
Diluted in /
5`)o FCI-XQ
2000N SO% seawater 1. 0.305 738.8314 18.766 0.021 no pits 0.5% CI-1A
Diluted in 1.5% 5% FCI-XCI-1A R
2000N 50% seawater 0.305 738.8314 18.766 0.021 no pits 0.
Diluted in I.5%FCI-XS
2000N 50% seawater 0.317 766.4377 19.468 0.021 no pits 0.5% C1-1A

Table #17 - Corrosion test results from tests conducted at 90 C for a period ranging for 6 hours with a coupon density of 7.86 g/cc having a surface area of 28.922 cm2 (coupons used were P110 steel) 61'..i.-.Av''' 'i -' _.' .:Wt-'10i µ, ,,-'!-;,-;:. 1 ,efir !
' lb 1t2 t .' ''''-' -'-' qA,,, -:;., ;:-;:is.-:!',"-...=:-''-' -' .# .,i. '.-, J''' ',` Artiir e . .-:- ' -!!r! , - -,! --, , , pidep404$
.',,_.-14, 4,,;õ 1,,,,,,,.., ,..--,:,-, - .-, - . - ,,:::444#14ge''il .,='--:-;.t",, ,:(e.,Y.,:,' '.11 ',''.--,,: -, -' '= ',' , r- ' ''--,,.'-...: . --: * r,- = '',.';::- . , tYPI,:4.-iX 1!: 'r,t'ZI :',.,4' T. ,, :t `. ' ' ,',',,,v - 4:',V..',--=
_ , '':..,{,,',i'; ii.1,_ ' -..---,',:', ..rf,'' '.---,, , '''''..4 '=
.,-. - - .SAi '''',-'' irr'-' Diluted in 50%
few pits on 2000N seawater 1.5% FCI-XP 0.388 981.3209 24.926 0.026 0.5% CI-IA side/back Diluted in 50% 1.5 few pits on % FCI-XQ
2000N seawater 0.5% CI-IA 0.589 1489.555 37.835 0.042 side/back Diluted in 50% few pits on 1.5% FCI-XR
2000N seawater 0.662 1674.896 42.542 0.047 side/back 0.5% C1-1A
-Diluted in 50% few pits on 1.5% FC1-XS
2000N seawater 5% CI-1A 0.376 951.2314 24.161 0.027 side/back 0.
, Table #18 - Corrosion test results from tests conducted at 90 C for a period ranging for 6 hours with a coupon density of 7.86 g/cc having a surface area of 41.4 cm2 (coupons used were 1018 steel) ;, .', , -,, , . -::, ,,,,,k7:.-.::,, ' ,..',-,,f --= ,,. , --, ' - , - ' '':, ..., ;
';'.-.:.1:. J=21. ,, -,,, :,=,j ..: '04iiiii),.
?'..81,044$:', . ,.&47`.`.1.j..` '- , .:;iiiiii ,, ':).V:i2 13;<Fi%I'414?'';ii.iffitii : '.:.`: . i ) -,µ; ;.,: ;::4-7,M.IF.,!03 . "- , - ,''''-' ' : õ=,'ip.fi.,'e.'.'-,:.:,'..
Diluted in 50%
15% HCI seawater 1% FCI-XP 0.135 239.3507 6.08 0.007 I% CI-1A
Diluted in 50% 1 FCI-XP
15% FICI seawater 0.5% C1-1A 0.206 364.0603 9.247 0.01 Diluted in 50%
0.75%CI- FCI-XP
15% HC1 seawater % 0.094 166.7506 4.235 0.005 Diluted in 50% - .
0.75% FCI-XP
15% HCI seawater 0.5% CI-1A 0.242 427.1217 10.849 0.012 Diluted in 50%
I %FC1-XQ
15% HCI seawater 1.173 2072.901 52.652 0.058 0.5% C1-1A
. ___________________ Diluted in 50% 10 FC1-XR
15% HC1 seawater 1.204 2126.07 54.002 0.06 0.5% CI-IA
Diluted in 50%
0.75% FCI-XQ
15% HCI seawater 1.022 1805.11 45.85 0.051 0.50/o C1-1A
Diluted in 50% 0.75% FCI-XR
15% HC1 0.801 1415.084 35.943 0.04 , 0.5% C1-1A

-seawater L
Table #19- Corrosion test results from tests conducted at 90 C for a period ranging for 6 hours with a coupon density of 7.86 Wee having a surface area of 41.4 cm2 (coupons used were 4140 steel) F-7 :
WtIas 1034 = '61 -,'".1P1&=;" , . :'"1! " !
Diluted in 50% 1% FCI-XQ
15% HC1 seawater 2.553 4510.215 114.559 0.126 0.5% CI-IA
Diluted in 50% 1 /9 FCI-XR
15% HC1 seawater 1.502 2653.171 67.391 0.074 0.5% CI-IA
Diluted in 50%
75% FCI-XQ
15% HC1 seawater 0. 5.411 9558.483 242.785 0.268 0.5% CI-1A
Diluted in 50%
0.75% FCI-XR 2.172 3837.03 97.461 15% 1-10 seawater 0.107 0.5% C1-1A
Diluted in 50%

15% HCI seawater 1 /0 FCI-XQ0.95 1677.221 42.601 0.047 1% CI-1A
Diluted in 50% =
0.75% FCI-XQ
15% HCI seawater 1.836 3242.628 82.363 0.091 1% CI-1A
Diluted in 50% 1% FCI-XP
15% HCI seawater 0.316 557.6606 14.165 0.016 1% CI-1A
Diluted in 50%
0.75% FCI-XP
15% 1-1C1 seawater 0.874 1543.856 39.214 0.043 1% C1-1A
Diluted in 50%
I% FCI-XS
15% HC1 seawater 0.154 272.3828 6.919 0.008 1% CI-IA
Diluted in 50%
15% HC1 seawater 0.75 %FCI-XS0.196 346.0428 8.789 0.01 0.75% CI-1A
Table no - Corrosion test results from tests conducted at 90 C for a period ranging for 6 hours with a 771: density of (,i;lupo.,:nHs, used were J55 steel) 'C, ' - -f ' õ
, 4410 , = - = = " :===
Diluted in 50% 1.5 /0 FCI-XP
HCR-2000N 0.135 340.3396 8.645 0.01 0.5% CI-IA

seawater Diluted in 50%
5% FCI-XQ
HCR-2000N seawater 1. 0.296 748.1908 --19.004 -- 0.021 0.5% CI-1A
Diluted in 50% 1.5% FCI-XR
HCR-2000N seawater 0.269 680.932 17.296 0.019 0.5% CI-1A
Diluted in 50% 1.5% FC1-XS
HCR-2000N seawater 0.5% C1-1A 0.252 638.1999 -- 16.21 -- 0.018 Table #21¨ Corrosion test results from tests conducted at 90 C for a period ranging for 6 hours with a coupon density of 7.86 Wee having a surface area of 30.199 cm' (coupons used were N80 steel) =
"dPutge - afir.
, __________________ 5V-z=sy.,- tfY, `,7, `:1`
Diluted in 50%
.5 1 /o F CI- XP
HCR-2000N seawater 0.188 455.7459 11.576 -- 0.013 0.5% CI-1A
Diluted in 50%
5% FCI-XQ
HCR-2000N seawater 1. 0.331 802.5196 20.384 0.022 0.5% CI-1A
Diluted in 50%
1.5% I -XRFC
HCR-2000N seawater 0.351 851.1939 21.62 -- 0.024 0.5% CI-1A
Diluted in 50% 1.5% FCI-XS
HCR-2000N seawater 0.298 721.3959 18.323 -- 0.02 0.5% CI-1A
Table 422 ¨ Corrosion test results from tests conducted at 90 C for a period ranging for 6 hours with a coupon density of 7.86 g/cc having a surface area of 30.199 cm2 (various steel coupons were used) -' __________________________________ urface . - 'CIL*Otsidoit":,A1040,S4V, = .=*illfrIltr ..110M4' n , Itasfyr -41,40 µ:..
Diluted HCR- in 50%
L80-13CR seawater 2.5% FCI-XP 0.028 8.47 244.3424 6.206 0.007 2000N 5% CI-1A
Diluted HCR- in 50% 5% FCI-XP
L80-13CR seawater 5% 0.022 8.47 185.6311 4.715 0.005 HCR- Diluted 5% FCI-XR
1,80-13CR
zOOON in 50% 5% CI-1A 0.019 8.47 161.4559 4.101 0.005 seawater =
Diluted HCR- in 50% 5% FCI-XQ
L80-13CR seawater 0.02 8.47 171.8167 4.364 0.005 2000N 5cY0 C1-1A
Diluted 14CR- in 50% 5% FCI-XS
L80-13CR 0.015 8.47 127.7833 3.246 0.004*
2000N seawater 5% CI-1A
Diluted HCR- in 50% 5% FCI-X0 L80-13CR 0.044 8.47 376.4426 9.562 0.011 2000N seawater 5% CI-1A
Diluted HCR- in 50%
seawater 1.5% FCI-XM
J55 0.294 28.922 743.8923 18,895 0.021 2000N 1% C1-1A
Diluted HCR- in 50% 1.5`)/0 FCI-XM
N80 0.363 30.199 878.0737 22.303 0.025 2000N seawater 1% Cl- 1 A
0.
355 15% HCI 75% FC1-XM0.308 28.922 777.7746 19.755 0.022 0.5Vo CI-1A
N80 15% HCI 0.75% FCI-XM0.98 30.199 2373.414 60.285 0.066 0.5% CI-1A
Diluted HCR- in 50% 1.5% FCI-XL
J55 0.117 28.922 295.079 7.495 0.008 2000N seawater 1% C1-1A
Diluted HCR- in 50% 1.5% FCI-XL
N80 0.156 30.199 377.5281 9.589 0.011 2000N seawater I% CI-IA
N80 15% HCI 1.5% FC1-XM0.238 30.199 577.3104 14.664 0.016 I% CI-1A
*no pits, but checkered surface Table #23 - Corrosion test results from tests conducted at 90 C for a period ranging for 6 hours with a coupon density of 7.86 glee :
Diluted in HCR- 5%
1018 50% seawater 1. FCI-XM0.338 41.4 597.5818 15.179 0.017 2000N I% CI-1A
Dil ute d in HCR- 2% FCI-XM
N80 2000N I% Cl- IA 50% seawater 0.196 30.199 475.6031

12.080 0.013 HCR- Diluted in 2% FCI-XM

2000N 1% CI-1A 0.191 28.922 482.9484 12.267 0.014 50% seawater Diluted in HCR- 2% FCI-XM
L80 2000N 1% C1-1A 50% seawater 0.305 30.199 738.8314 18.766 0.021 Diluted in HCR- 1.5% FCI-XL

N80 50% seawater 10/ CI-1A 0,148 30.199 357.9131 9.091 0.010 Diluted in HCR- 1.5% FCI-XL

J55 50% seawater 1 %C1-1A 0.115 28.922 290.0219 7.367 0,008 Diluted in HCR- 5% FCI-XL
L80 50% seawater 1. 0.115 30.199 278.2423 7.067 0.008 2000N 1% CI-IA
Additionally, corrosion inhibition packages according to preferred embodiments of the present invention will allow the end user to utilize synthetic and modified acids that have down-hole performance advantages, transportation and storage advantages as well as the health, safety and environmental advantages. The person skilled in the art will also understand that the corrosion package according to the present invention is useful when as also utilized with conventional acid systems.
In addition to stability at high temperatures and desirable corrosion rates as discussed above, the use of synthetic and modified acids along with a corrosion package according to a preferred embodiment of the present invention, allows for reduction in skin corrosiveness, a more controlled or methodical spending or reacting property, minimizing near well bore damage typically caused by an ultra-aggressive reaction with the formation typically caused by HCI and increasing formation penetration providing superior production overtime.
USES OF CORROSION INHIBITION PACKAGES ACCORDING TO PREFERRED
EMBODIMENTS OF THE PRESENT INVENTION
The uses (or applications) of the corrosion inhibition packages according to the present invention when combined (or mixed) with acidic compositions upon dilution of the latter ranging from approximately I
to 90% dilution, include, but are not limited to: injection/disposal well treatments; matrix acid squeezes, soaks or bullheads; acid fracturing, acid washes; fracturing spearheads (breakdowns); pipeline scale treatments, cement breakdowns or perforation cleaning; pH control; and de-scaling applications. As would be understood by the person skilled in the art, the methods of use generally comprise the following steps:
providing a composition comprising a corrosion inhibitor package according to a preferred embodiment of the present; mixing said package with an acid composition; exposing a surface (such as a metal surface) to the acid composition comprising the package; allowing the acid composition a sufficient period of time to act upon said surface; and optionally, removing the acid composition when the exposure time has been determined to be sufficient for the operation to be complete or sufficiently complete. Another method of use comprises: injecting the acid composition comprising the package into a well and allowing sufficient time for the acid composition to perform its desired function. Yet another method of use comprises: exposing the acid composition comprising the package to a body of fluid (typically water) requiring a decrease in the pH
and allowing sufficient exposure time for the acid composition to lower the pH
to the desired level.
One of the advantages of the use of a synthetic acid composition using a corrosion inhibition package according to a preferred embodiment of the present invention includes:
the reduction of the total loads of acid, and the required number of tanks by delivering concentrated product to location and diluting with fluids available on location (with low to high salinity production water).
While the foregoing invention has been described in some detail for purposes of clarity and understanding, it will be appreciated by those skilled in the relevant arts, once they have been made familiar with this disclosure that various changes in form and detail can be made without departing from the true scope of the invention in the appended claims.

Claims (35)

1 . A corrosion inhibition package for use with an aqueous acid composition, said package comprising:
a terpene; a cinnamaldehyde or a derivative thereof; at least one amphoteric surfactant; and a solvent.

2. The corrosion inhibition package as claimed in claim 1, wherein the terpene is selected from the group consisting of: citral; carvone; ionone; ocimene; cymene; and combinations thereof.

3. The corrosion inhibition package as claimed in claim 1 or 2, wherein the at least one amphoteric surfactant is selected from the group consisting of: a sultaine surfactant; a betaine surfactant; and combinations thereof.

4. The corrosion inhibition package as claimed in claim 3, wherein the sultaine surfactant and betaine surfactant are selected from the group consisting of: an amido betaine surfactant; an amido sultaine surfactant; and combinations thereof.

5. The corrosion inhibition package as claimed in claim 4, wherein the amido betaine surfactant and is selected from the group consisting of: an amido betaine comprising a hydrophobic tail from C8 to C16.

6. The corrosion inhibition package as claimed in claim 5, wherein the amido betaine surfactant comprising a hydrophobic tail from C8 to C16 is cocamidobetaine

7. The corrosion inhibition package as claimed in claim 1 to 6, further comprising an anionic surfactant.

8. The corrosion inhibition package as claimed in claim 7, wherein the anionic surfactant is a carboxyl ic surfactant.

9. The corrosion inhibition package as claimed in claim 8, wherein the carboxylic surfactant is a dicarboxylic surfactant.

10. The corrosion inhibition package as claimed in claim 9, wherein the dicarboxylic surfactant comprises a hydrophobic tail ranging from C8 to C16.

11. The corrosion inhibition package as claimed in claim 10, wherein the dicarboxylic surfactant is sodium lauriminodipropionate

12. The corrosion inhibition package as claimed in any one of claims 1 to 11, wherein the surfactant is selected from the group consisting of: cocamidopropyl betaine; B-Alanine, N-(2-carboxyethyl)-N-dodecyl-, sodium salt (1:1); and a combination thereof.

13. The corrosion inhibition package as claimed in any one of claims 1 to 12, wherein the solvent is selected from the group consisting of: isopropanol; methanol; ethanol; 2-butoxyethanol; diethylene glycol;;
and combinations thereof.

14. The corrosion inhibition package as claimed in any one of claims 1 to 13, wherein the terpene is present in an amount ranging from 5% to 30% by volume of the total volume of the corrosion inhibition package.

15. The corrosion inhibition package as claimed in any one of claims 1 to 14, wherein the cinnamaldehyde or derivative thereof is present in an amount ranging from 5%
to 30% by volume of the total volume of the corrosion inhibition package.

16. The corrosion inhibition package as claimed in any one of claims 1 to 15, wherein the at least one surfactant is present in an amount ranging from 2% to 20% by volume of the total volume of the corrosion inhibition package.

17. The corrosion inhibition package as claimed in any one of' claims 1 to 16, wherein the solvent is present in an amount ranging from 25% to 80% by volume of the total volume of the corrosion inhibition package.

18. The corrosion inhibition according to claim 17, wherein the solvent is present in an amount ranging from 25% to 75% by volume of the total volume of the corrosion inhibition package.

19.. A liquid acidic composition comprising:
- an acidic solution;
- a corrosion package comprising:
- a terpene;
- a cinnamaldehyde or a derivative thereof;

- at least one amphoteric surfactant; and - a solvent;
wherein the volume % of the corrosion package in the acidic composition ranges from 0.1 to 10%.

20. The liquid acidic composition according to claim 19, further comprising a metal iodide or iodate.

21 The liquid acidic composition according to claim 20, wherein the volume % of the metal iodide or iodate in the acidic composition ranges from 0.1 to 1.5%.

22 The liquid acidic composition according to any one of claims 18 to 21, wherein the acid is selected from the group consisting of: mineral acids, organic acids, synthetic acids;
modified acids; complexed acids and combinations thereof.

23. The liquid acidic composition according to any one of claims 18 to 22, wherein the acid solution is selected from the group consisting of HCI, Lysine-HCI, Urea-HCl, hydrofluoric acid, sulfuric acid, methanesulfonic acid, methanesulfonic acid-Urea, phosphoric acid; phosphoric acid-urea; and p-toluene sulfonic acid.

24. The liquid acidic composition according to any one of claims 18 to 23, wherein the metal iodide or iodate selected from the group consisting of: cuprous iodide; potassium iodide, sodium iodide; lithium iodide and combinations thereof.

25. The liquid acidic composition according to claim 24, wherein the metal iodide is potassium iodide.

26. The liquid acidic composition according to claim 25, wherein the potassium iodide is present in an amount ranging from 0 1 to 1 5% vol./vol of the acidic composition.

27 The liquid acidic composition according to claim 26, wherein the potassium iodide is present in an amount ranging from 0.25 to 1.25 % vol./vol of the acidic composition

28. The liquid acidic composition according to claim 26, wherein the potassium iodide is present in an amount of 1% by vol./vol. of the acidic composition

29. An aqueous synthetic or modified acid composition for use in offshore oil and gas operations, said composition comprising:
- lysine and hydrochloric acid in a molar ratio of not less than 1:12;
- a surfactant;
- a corrosion inhibition package; and - an intensifier.

30. An aqueous synthetic or modified acid composition for use in offshore oil and gas operations, said composition comprising:
- lysine and hydrochloric acid in a molar ratio of not less than 1:12;
- a corrosion inhibition package; and - an intensifier

31. The composition according to claim 29 or 30, wherein said corrosion inhibitor comprises:
- a terpene;
- a cinnamaldehyde or a derivative thereof;
- at least one amphoteric surfactant; and - a solvent.

32. The use of a corrosion inhibitor package with an acidic composition where the acidic composition comprises an acid selected from the group consisting of: a mineral acid; an organic acid; a modified acid; a complexed acid or a synthetic acid, said corrosion inhibitor package comprising:
- a terpene;
- a cinnamaldehyde or a derivative thereof;
- at least one amphoteric surfactant; and - a solvent.

33. The use according to claim 32, where the at least one amphoteric surfactant is selected from the group consisting of: a sultame surfactant and a betaine surfactant; and combinations thereof.

34. The use according to any one of claims 32 and 33, further comprising an anionic surfactant.

35. The use of a liquid acidic composition according to any one of claims 18 to 28 in the oil industry to perform an activity selected from the group consisting of: stimulating formations; assisting in reducing breakdown pressures during downhole pumping operations; treating wellbore filter cake post drilling operations; assisting in freeing stuck pipe; descaling pipelines and/or production wells; increasing injectivity of injection wells; lowering the pH of a fluid; fracturing wells;
performing matrix stimulations;
conducting annular and bullhead squeezes & soaks; pickling tubing, pipe and/or coiled tubing; increasing effective permeability of formations; reducing or removing wellbore damage;
cleaning perforations, solubilizing limestone, dolomite, and calcite; and scale removal from a surface selected from the group consisting of: equipment, wells and related equipment and faciiities.